Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982799Generated: November 2, 2026

Benzyl Bromide → 4-(3-Benzyloxypropyl)bromobenzene

https://huagongshe.com/reaction/1982799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(4-Bromophenyl)propan-1-olHCID 10560614—
SolventBenzeneHCID 241—
Product4-(3-Benzyloxypropyl)bromobenzeneHCID 21909326—

Reaction Steps

A suspension of sodium hydride (60%, 0.97 g), 3-(4-bromophenyl)-1-propanol (1.0 g) and benzyl bromide (0.69 mL) in benzene (24 mL) was stirred under reflux for 7 hours. After cooling to room temperature, a saturated aqueous ammonium chloride solution (50 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (100 mL). The organic layer was washed with water (40 mL) and brine (40 mL) and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=20/1) to give 4-(3-benzyloxypropyl)bromobenzene (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541341B2
Source datasetuspto-grants-2009_06
ORD IDord-e8c78533f17249429c6555648473159e
Source noteuspto-grants-2009_06